NC_000009.12:g.(?_286441)_(289601_?)delRat Genome Database

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Variant : CV459168 (NC_000009.12:g.(?_286441)_(289601_?)del) Homo sapiens

Symbol: CV459168
Name: NC_000009.12:g.(?_286441)_(289601_?)del
RGD ID: 13485472
Condition: Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive [RCV000553243]
Clinical Significance: pathogenic|likely pathogenic
Last Evaluated: 11/06/2017
Review Status: criteria provided, single submitter
Related Genes: DOCK8  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_286441)_(289601_?)del
NC_000009.11:g.(?_286441)_(289601_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh389286,441 - 289,601CLINVAR
GRCh379286,441 - 289,601CLINVAR
Cytogenetic Map99p24.3CLINVAR
Trait Synonyms: AR hyperimmunoglobulin E syndrome; HIES autosomal recessive; Hyper Ig E syndrome, autosomal recessive; HYPER-IgE RECURRENT INFECTION SYNDROME 2, AUTOSOMAL RECESSIVE



Disease Annotations     Click to see Annotation Detail View

Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000553243 CLINVAR
MedGen C4722305 CLINVAR
NCBI Gene DOCK8 CLINVAR
OMIM 243700 CLINVAR
  611432 CLINVAR